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组胺 H2 受体在变应原特异性免疫治疗中的免疫调节作用:变应性鼻炎的小鼠模型。

Immunomodulatory role of histamine H2 receptor in allergen-specific immunotherapy: a mouse model of allergic rhinitis.

机构信息

Department of Otolaryngology-Head and Neck Surgery, College of Medicine, the Catholic University of Korea, Seoul, Korea.

出版信息

Otolaryngol Head Neck Surg. 2011 Apr;144(4):500-5. doi: 10.1177/0194599810392154. Epub 2011 Feb 1.

DOI:10.1177/0194599810392154
PMID:21493224
Abstract

OBJECTIVE

The purpose of this pilot study was to investigate the effects of HR2 on allergen-specific immunotherapy in a mouse model of allergic rhinitis.

STUDY DESIGN

An in vivo study using an animal model.

SETTING

Catholic Research Institutes of Medical Science.

METHODS

Fifty mice were divided into 5 groups: control, allergic rhinitis (AR), immunotherapy (IT), immunotherapy with HR2 agonist (HI), and immunotherapy with HR2 antagonist (HB). All mice except for the control group were sensitized with ovalbumin (OVA). After 1 week, mice in the IT, HI, and HB groups underwent immunotherapy by intradermal injections of OVA. During immunotherapy, the HI group was injected with HR2 agonist, whereas the HB group was injected with HR2 antagonist. All sensitized mice were challenged with intranasal OVA. After the final challenge, allergic behavior was evaluated. Interleukin (IL)-13, interferon-γ, IL-10, and transforming growth factor (TGF)-β levels in nasal lavage fluid (NALF), as well as OVA-specific IgE levels in serum, were measured. The number of eosinophils in lamina propria was evaluated.

RESULTS

The levels of serum OVA-specific IgE and IL-13 in NALF were significantly increased in the HB group compared with the IT group (P < .05). Also, the tissue eosinophil counts were higher in the HB group than in the IT group (P < .05).

CONCLUSION

HR2 antagonist impaired OVA-specific immunotherapy in mice. Although confirmation of this preliminary result is needed, these findings suggest that HR2 receptors may have inhibitory effects on immune tolerance. The authors suggest that application of this property could enhance the efficiency of allergen-specific immunotherapy.

摘要

目的

本初步研究旨在探讨 HR2 对变应性鼻炎小鼠模型中变应原特异性免疫治疗的影响。

研究设计

采用动物模型的体内研究。

设置

天主教医疗科学研究所。

方法

将 50 只小鼠分为 5 组:对照组、变应性鼻炎(AR)组、免疫治疗(IT)组、HR2 激动剂免疫治疗(HI)组和 HR2 拮抗剂免疫治疗(HB)组。除对照组外,所有小鼠均用卵清蛋白(OVA)致敏。致敏 1 周后,IT、HI 和 HB 组小鼠通过皮内注射 OVA 进行免疫治疗。在免疫治疗期间,HI 组注射 HR2 激动剂,而 HB 组注射 HR2 拮抗剂。所有致敏小鼠均接受鼻内 OVA 挑战。最后一次挑战后,评估过敏行为。测量鼻洗液(NALF)中白细胞介素(IL)-13、干扰素-γ、IL-10 和转化生长因子(TGF)-β水平以及血清中 OVA 特异性 IgE 水平。评估固有层中嗜酸性粒细胞的数量。

结果

与 IT 组相比,HB 组 NALF 中血清 OVA 特异性 IgE 和 IL-13 水平显著升高(P<0.05)。此外,HB 组组织嗜酸性粒细胞计数高于 IT 组(P<0.05)。

结论

HR2 拮抗剂削弱了小鼠的 OVA 特异性免疫治疗。尽管需要确认这一初步结果,但这些发现表明 HR2 受体可能对免疫耐受具有抑制作用。作者建议应用这一特性可以提高变应原特异性免疫治疗的效率。

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